Cardiac Toxicity Associated with Immune Checkpoint Inhibitors: A Systematic Review

Simple Summary This review article addresses the toxic effects on the heart associated with the use of certain cancer-treating drugs known as immune checkpoint inhibitors. These drugs target specific proteins in the cell cycle that are abundantly expressed in cancerous cells; however, they inadvertently damage non-cancerous tissue. In the heart, this occurs in the form of dysfunction or death of smooth muscle cells, leading to consequences such as infection, heart rhythm changes, and hormonally dependent and independent ischemia. This review examines the average and median onset of these drug toxicities as well as antidotes. One key observation is that these side effects are positively skewed, meaning they occur early in cancer treatment. Abstract Immune checkpoint inhibitors are immune stimulatory drugs used to treat many types of cancer. These drugs are antibodies against inhibitory proteins, such as CTLA-4 and PD-1/PD-L1, that are expressed on immune cells. When bound, they allow for increased stimulation of T cells to fight tumor cells. However, immune checkpoint inhibitors have several immune-related adverse effects. Many cases have come to light recently of cardiotoxicity as a result of treatment with these drugs. Cardiotoxicity from immune checkpoint inhibitors is unique due to its rarity and high mortality rate. Patients with this toxicity may present with myocarditis, pericarditis, Takotsubo cardiomyopathy, conduction disorders, and others within just a few weeks of starting immune checkpoint inhibitors. We present here a review of the current research on immune checkpoint inhibitors, their associated cardiotoxicities, the timing of presentation of these conditions, lab tests and histology for each condition, and finally the treatment of patients with cardiotoxicity. We observe a positive skew in the onset of presentation, which is significant for the treating physician.


Introduction
In the last several years, immune checkpoint inhibitors (ICIs) have become the backbone of the treatment plan in many types of cancer. Tumor cells express neoantigens, mutated proteins that immune cells can recognize as foreign and destroy; however, many tumors also express factors that inhibit the immune system, thus allowing them to grow undetected in the body [1]. Immune checkpoint inhibitors work by blocking the inhibitory signals from tumor cells to T cells that recognize them, thus allowing the tumor cells to be destroyed by the patient's own immune system. The first ICI was approved by the FDA in 2011 [2], and since then several different ICIs against a variety of targets have and the type of cancer being treated. Trends were enumerated qualitatively through a table and a graph.

General
Cardiotoxicity is a very rare complication of immune checkpoint inhibitors, affecting up to 1% of patients; this percentage is higher in patients taking a combination of ICIs [11]. Others have argued that the total risk of cardiac events in patients with ICI therapy is much higher, from 3.1% [12] to 9.7% [13]. This discrepancy may be due to misclassification and difficult diagnosis of cardiac events caused by ICIs, especially during the current COVID-19 pandemic [14]. The most common presentation of cardiotoxicity due to ICIs is myocarditis ( Table 1). High-dose corticosteroids [17,23,26] Arrhythmias and conduction disorders Unknown Unknown ECG changes High-dose corticosteroids, supportive [17,18,22] Myocardial infarction Unknown Chest pain and shortness of breath ECG changes, troponin, and others Cardiac catheterization, supportive [17] Abbreviations: ICI, immune checkpoint inhibitor; NT-proBNP, N-terminal -prohormone brain natriuretic peptide; CMR, cardiovascular magnetic resonance imaging; ECG, electrocardiogram; NSAIDs, non-steroidal anti-inflammatory drugs.
Patients can have a wide range of signs and symptoms, from asymptomatic to severe chest pain, dyspnea, multiorgan failure, and sudden death [27] (Appendix A). These symptoms usually begin within the first 3 months of starting immunotherapy, but they can also start up to a year after therapy finishes [27]; the average time until symptoms start varies between the treatment (Table 2), the patient's cancer (Table 3, Figure 1), and the type of cardiotoxicity (Table 4, Figure 2).   Table 4. Weeks until ICI-associated cardiotoxicity, organized by treatment and type of cardiotoxicity.
Reinforcing the idea that T cells are the primary mediators of cardiotoxicity with ICIs, a remarkable study by Wang et al. shows that fatal myocarditis was developed in mice genetically predisposed to systemic autoimmunity due to PD-1 deficiency [31]. However, in mice, the myocarditis was caused by CD4+ and CD8+ T cells as well as autoantibodies against cardiomyocytes. Mice with a genetic predisposition to autoimmunity but without a PD-1 deficiency did not develop myocarditis, demonstrating that prevention of myocarditis is likely mediated by PD-1 [31]. Love et al. found in a similar study that CTLA-4 removal on T cells also caused severe myocarditis in mice, but lack of IL-12 prevented CD8+ T cells from proliferating, thus ameliorating the myocarditis [32]. PD-L1 expressed in the human myocardium is involved in protecting immune-mediated cardiac injury and inflammation [29].
Autoantibodies have been postulated to lead to cardiotoxicity in patients treated with ICIs. A case described by Martinez-Calle et al. showed that the patient did have IgG autoantibodies against cardiac troponin T, but it is unknown if the antibodies were present before initiation of ICI therapy [33]. Two other patients have shown autoantibody deposition in cardiac muscle, suggesting a direct relationship between the antibodies and myocarditis [34]. However, many more cases have stated that no autoantibodies were found on histology or blood tests [11,15,35], leading to the conclusion that autoantibodies are generally not involved in the pathogenesis of cardiotoxicity with ICIs.

Myocarditis
Myocarditis, or inflammation of the myocardial muscle, is the most common form of cardiotoxicity caused by ICIs. It is also the most fatal form of cardiotoxicity, with a mortality rate of up to 50% [16,36,37]. It was first recognized as an IRAE during clinical trials, and as use of ICIs has increased, awareness has also increased.
Myocarditis can develop as early as 2 weeks after starting ICI therapy [17]; however, the median amount of time after beginning ICI treatment that patients experience symptoms is 65 days [18]. Eighty-one percent of patients present within 3 months of initiation of therapy [17]. Patients with ICI-associated myocarditis can present with a wide range of symptoms. Most commonly, patients will have a primary complaint of shortness of breath [15,19]. Palpitations and signs of congestive heart failure, such as edema, fatigue, weakness, or wheezing, are also common symptoms [18].
On lab tests, patients will often experience elevation of BNP or NT-proBNP, signs of active inflammation such as elevated CRP and hepcidin, and elevated troponin and CK-MB [17,20]. Troponin is an important predictor of the patient's risk of a major adverse cardiac event (MACE), which is defined as cardiovascular death, cardiac arrest, complete heart block, or cardio-genic shock [11,37]. Troponin I is the most useful troponin for this purpose; troponin T may be elevated with concurrent myositis, reducing its usefulness [37]. Patients who do not have an elevated troponin I almost never have myocarditis, making it a very sensitive tool, though it is not specific [38]. NT-proBNP is less specific for myocarditis and can be elevated due to cancer-related inflammation rather than ICI-associated cardiotoxicity [16,39]. An abnormal ECG is also common but is not always present [17].
The gold standard to diagnose myocarditis is endomyocardial biopsy [40,41]. The biopsy needs to be taken from about six regions because the area of inflammation is localized to specific regions in the heart [21,40]. Patients have been reported to have a wide range of histological findings suggestive of myocarditis. As stated earlier, autoantibodies are almost never found in these patients [15]. Histopathological evaluation of endomyocardial biopsies has revealed a lymphocytic infiltrate of CD4+ and CD8+ cells in the myocardium and conducting system of patients with myocarditis [11,19]. There may also be fibrosis without granulomas or histiocytes [17,26]. These T cell populations are clonally similar to those found in tumors as well, suggesting that cardiotoxicity is caused by antigen similarity; however, it may also be caused by reduced inhibition of self-reactive T cells [27]. PD-L1 is also highly expressed in the myocardium of these patients [19]. One of the youngest cases of pembrolizumab-induced myocarditis, described by Läubli et al. [42], similarly demonstrated predominant infiltration of CD8+ cells on myocardial biopsy. These findings seem to indicate that the cardiotoxicity is T-cell-mediated rather than antibody-mediated.
However helpful endomyocardial biopsy may be, this procedure is invasive and not routinely performed. A cardiac magnetic resonance scan (CMR) is also very effective and is the gold standard of imaging for myocarditis [21]. On CMR, patients will have active inflammation with increased capillary permeability, possible myocardial ischemia, and late gadolinium enhancement [17,21]. If CMR is unavailable, PET/CT is a good alternative [22].
Several studies have found that patients who receive combination ICI therapy, most commonly ipilimumab and nivolumab, have an increased risk of developing myocarditis as compared to patients only taking one ICI [6,16,39,43,44]. Zhang et al. also report that there is an increased risk of myocarditis with the female sex and older age [6]; other studies disagree, saying that there is no age association and higher risk with the male sex [16,43]. This discrepancy may be due to the fact that cardiac-adverse events have been more commonly reported in male patients than female patients in the past, since females have often been less represented in clinical trials [43]. There is no association of myocarditis with a specific type of cancer [36]. In addition, there is an increased risk of ICI-associated myocarditis with hypertension; tobacco use; and the use of prescription statins, ACE inhibitors, and angiotensin inhibitors [23]. Up to half of all patients with ICI-associated myocarditis will present with other, concurrent IRAEs [23,44]; in particular, up to 25% of patients with myocarditis may have concomitant myositis, and 10% may have concomitant myasthenia gravis [36].
Interestingly, a study by Awadalla et al. shows that patients receiving ICI therapy may have a lower likelihood of developing myocarditis when they have been vaccinated for influenza [45]. The study's results show that patients with myocarditis were less likely to have received the flu vaccine; in addition, vaccinated patients who did develop myocarditis had lower serum troponin levels and were less likely to have a MACE [45].
PD-1 expression is constitutive in the myocardium and is important for normal immune function, so inhibition of this pathway can lead to severe issues [46]. In one study, Wang et al. showed that PD-1 deficiency in mice causes them to develop fatal autoimmune myocarditis, almost always within 10 weeks after birth [31]. Myocarditis did not develop in mice with a deficiency in immune-regulating molecules not in the PD-1/PD-L1 pathway [31]. However, Love et al. showed that myocarditis can also develop in mice deficient in CTLA-4 [32]. In humans, patients with myocarditis often have high expression of PD-L1 in cardiac tissue, suggesting that PD-L1 is used by the heart to prevent inflammation [37].

Pericarditis
Pericardial disease, or inflammation of the pericardial sac surrounding the heart, is another common form of cardiotoxicity, with an incidence of 0.3% [24,47]. This includes pericarditis, pericardial effusion, and even clinical tamponade [17]. Though it is not as fatal as myocarditis, it has a mortality rate of 13-21% [6,16,19,48]. On average, patients who develop pericarditis do so within 30 days of starting ICI treatment [16], but several cases have been described where pericarditis was diagnosed several months after starting treatment [35,[49][50][51]. Often, patients will present with chest pain, shortness of breath, and hemodynamic instability after ICI therapy [16,24]. Shortness of breath is the most common symptom on presentation [23].
Patients will frequently show ECG changes during pericardial disease [16]. In addition, pericardial effusion or thickening may be seen on CT scan, and CMR will show pericardial inflammation and/or fibrosis [25]. Analysis of pericardial effusion fluid shows lymphocytes and plasma cells without evidence of malignant cells or microorganisms causing the symptoms [17,25,50]. There may also be a hemorrhage or fibrinous exudate present [25]. Pericarditis has rarely been reported to occur in conjunction with myocarditis [44,52]; a normal troponin level can rule out this possibility.
Several studies have shown that there is a higher risk of pericardial disease when ICIs are given for non-small-cell lung cancer (NSCLC) [17,39,47,48,53]. It is hypothesized that this could be due to the use of radiotherapy in lung cancer in addition to ICIs, which exposes more shared antigens [39,50]; however, other studies argue that pericardial diseases are also common complications of certain cancers, thus inflating the significance of this result [48]. In addition, pericarditis is more common in males, but there is no increased risk with age [16,22,53]. Inno et al. found that treatment with anti-PD-1 or anti-PD-L1 therapy is more associated with pericardial disease than anti-CTLA-4 therapy [53]. Patients with pericarditis will frequently display other IRAEs in addition to pericarditis, such as hyperor hypothyroidism, arthritis, or hepatitis [35,50].
Interestingly, Altan et al. demonstrated that T cells infiltrating the pericardium had lower granzyme B expression present, indicating that perhaps cytotoxic granules are not causing pericardial inflammation and damage [25]; instead, this damage may be due to cytokine production. Antibodies are not involved in pathogenesis of this condition [35].

Takotsubo Cardiomyopathy
Takotsubo cardiomyopathy is a form of stress-induced cardiomyopathy that is an uncommon presentation of ICI-associated cardiotoxicity. Patients often begin having symptoms between 15 weeks and 8 months into treatment [17]. It presents as transient cardiac regional wall motion abnormalities, new ECG changes, and elevated troponin and NT-proBNP [17,26]. Clinicians may also see an apical ballooning pattern on echocardiogram [23].
Takotsubo cardiomyopathy may be caused by a direct effect of ICIs; however, it may also be caused by a sudden release of large amounts of catecholamines [44]. In addition, it may be a result of delayed cardiotoxicity from previous rounds of chemotherapy in patients who have not received ICIs as first line therapy [44]. As this is a relatively uncommon cardiotoxicity, there has not been much research on this presentation to date, and the cause is undetermined in the majority of cases.

Conduction Diseases
Conduction diseases caused by ICIs can include atrial fibrillation, ventricular tachycardia or fibrillation, and atrioventricular conduction disorders [17]. These diseases may come in conjunction with myocarditis or may appear separately. All conduction diseases are associated with increased mortality [17,18]; they can frequently cause sudden death as well [39]. The most common conduction disorder is atrial fibrillation [22].
It is unknown what causes conduction disease, but local inflammation or fibrosis may play a role. Other hypotheses include an electrolyte imbalance or non-inflammatory left ventricular dysfunction [22]. Lyon et al. argues that systemic inflammation caused by cancer and ICI treatment may also worsen cardiovascular conditions, leading to arrhythmias [44].

Myocardial Infarction
This extremely rare cardiac complication has been seen in atezolizumab and pembrolizumab treatment. The exact cause of this cardiotoxicity manifestation is unknown, but Chen et al. hypothesize that it may be due to rupture of atherosclerotic plaques seen in chronic inflammatory conditions, coronary spasm, or direct activation of T cells, leading to coronary vasculitis [17]. In addition, a myocardial infarction may be a result of previous cardiac arrhythmias caused by the ICI treatment combined with the hypercoagulability that is seen in patients with advanced cancer.

Ipilimumab
Ipilimumab is a fully human recombinant antibody against CTLA-4 [54]. It was initially approved by the FDA in 2011 and is now used for treatment of multiple cancers, including melanoma, renal cell carcinoma, colorectal cancer, hepatocellular carcinoma, and non-small-cell lung cancer [55] (Table 5). There are no contraindications [55]. Because ipilimumab works by stimulating the immune system, patients do not experience common cytotoxic chemotherapy side effects such as bone marrow suppression; instead, immune-related adverse events develop in up to 90% of patients [8]. The most common adverse effects patients experience while taking ipilimumab include fatigue, diarrhea, pruritis, rash, and colitis; severe immune-related reactions include enterocolitis, hepatitis, dermatitis, neuropathy, and endocrinopathy; it is seen in less than 1% of patients [55]. Ipilimumab very rarely causes cardiotoxicity. These IRAEs are dose-dependent and often happen within the first 3 months of the start of treatment [8]. If a patient experiences a severe IRAE, most physicians recommend permanent discontinuation of the drug. For more minor side effects, the drug may be withheld until the patient improves, but afterward, the patient can continue treatment [55,56].

Pembrolizumab
Pembrolizumab is a humanized IgG4 antibody against PD-1 [57]. This antibody does not trigger antibody-dependent cellular cytotoxicity, unlike normal IgG antibodies [10]. It was initially approved by the FDA in 2014 and is currently approved for treatment of many cancers, including melanoma, lung cancer, several types of squamous cell cancer, several types of lymphomas, urothelial carcinoma, any cancer that is high in microsatellite instability or is mismatch-repair-deficient, gastric and esophageal cancer, cervical cancer, hepatocellular carcinoma, Merkel cell carcinoma, renal cell carcinoma, endometrial carcinoma, tumor mutational burden high cancer, and triple-negative breast cancer (Table 5) [58].
Similar to ipilimumab, pembrolizumab commonly causes immune-related adverse events rather than cytotoxic effects, seen in up to 70% of patients [8]. These events can be severe or even fatal and happen in any body system or organ [58]. The most common adverse events experienced by patients are fatigue, musculoskeletal pain, decreased appetite, diarrhea, rash, fever, cough, constipation, nausea, abdominal pain, and pruritis [58]. Rarely, pembrolizumab can cause cardiotoxicity such as myocarditis and pericarditis, but this occurs in less than 1% of patients [58].

Nivolumab
Nivolumab is a fully human IgG4 antibody against PD-1 [59]. Similar to pembrolizumab, it does not work in the pathway of antibody-dependent cellular cytotoxicity [10]. It was initially approved by the FDA in 2014 and is now approved for treatment of many cancers, including melanoma, non-small-cell lung cancer, malignant pleural mesothelioma, renal cell carcinoma, classical Hodgkin lymphoma, squamous cell carcinoma of the head and neck, urothelial carcinoma, colorectal cancer, hepatocellular carcinoma, and esophageal squamous cell carcinoma (Table 5) [60].
In patients, nivolumab can cause a number of side effects related to immune cell overactivation, which can be severe. The most common adverse effects seen are fatigue, rash, pruritis, and diarrhea [1]; other common symptoms include musculoskeletal pain, nausea, vomiting, abdominal pain, constipation, cough, dyspnea, asthenia, upper respiratory tract infections, fever, and headache [60]. These IRAEs can develop very late after finishing ICI treatment because a single administration of nivolumab can cause inactivation of PD-1 molecules for almost 3 months [61]. Cardiac adverse effects have been seen in less than 1% of patients [60].
Ipilimumab is often administered with nivolumab for treatment of advanced renal cell carcinoma, microsatellite instability-high or mismatch repair deficient metastatic colon cancer, hepatocellular carcinoma, and metastatic non-small-cell lung cancer (even if PD-L1 expression is less than 1%) [55,62]. However, side effects of this combination can be severe, leading to discontinuation of therapy in up to 40% of patients [46]. Though cardiotoxicity is still rare, combination ipilimumab and nivolumab therapy has a higher incidence of cardiac-adverse effects than either treatment alone [11].

Atezolizumab
Atezolizumab is a humanized IgG mouse antibody against PD-L1 [63]. It was initially approved by the FDA in 2016 and has since been approved for urothelial carcinoma, nonsmall-cell lung cancer, triple-negative breast cancer, small-cell lung cancer, hepatocellular carcinoma, and melanoma (Table 5) [64]. The most common reported adverse effects include fatigue, nausea and vomiting, cough, dyspnea, decreased appetite, alopecia, constipation or diarrhea, headache, and rash; the specific side effects vary based on the cancer being treated [64]. Myocarditis or pericarditis are less common side effects occurring in less than 1% of patients; for any grade severity of cardiotoxicity, the drug is recommended to be permanently discontinued [63,64]. To the best of our knowledge, only one case has been reported in the literature about cardiotoxicity using atezolizumab specifically [65]. More case reports may be seen in the future as this drug continues to be used more frequently as a first-line biologic agent.

Durvalumab
Durvalumab is a fully human IgG antibody against PD-L1 that was initially approved by the FDA in 2017 [66,67]. It is indicated for the treatment of urothelial carcinoma after platinum-containing therapy and non-small-cell lung cancer (Table 5) [66]. The most common side effects reported include fatigue, constipation, urinary tract infections, edema, pneumonitis, dyspnea, rash, cough, and nausea, depending on the patient's cancer type [66]. More severe side effects include hyperthyroidism or hypothyroidism, colitis, diarrhea, and hepatitis, which can be fatal [67]. With high-grade side effects, the drug may need to be permanently discontinued, but usually the drug only needs to be halted or the dose lowered [67]. Cardiotoxicity for this drug is very rare and has only been reported in three cases by name [19,20,38]. Expanded use of this drug may reveal more significant cardiotoxicity in the future.

Antidotes for ICI-Associated Cardiotoxicity
The most frequently recommended treatment for ICI-associated cardiotoxicity is highdose corticosteroids [68,69]. Especially for myocarditis, higher doses of corticosteroids have been associated with better outcomes for patients [20]. Patel et al. recommend that patients receive 1000 mg/day of corticosteroids initiated within 24 h of presentation; after resolution of symptoms, steroids should be tapered over at least 4-6 weeks [23].
However, there have also been cases of cardiotoxicity that are refractory to steroids. In these cases, Brahmer et al. recommend cardiac transplant rejection medications, including mycophenolate mofetil, infliximab, or anti-thymocyte globulin [68]. However, infliximab cannot be given to patients with heart failure [6]. In addition, other symptom-based treatments are often used, such as anti-coagulants, beta blockers or ACE inhibitors in heart failure, amiodarone with arrhythmias, and pericardiocentesis or pericardial window placement in cardiac tamponade [22]. For pericarditis specifically, Waliany et al. recommend that NSAIDs and colchicine are also effective in treating signs and symptoms [7].
Several studies have recommended that even after minor grade cardiotoxicity, ICIs need to be discontinued temporarily; in high-grade toxicities, they must be permanently discontinued [56]. However, ICIs have a long half-life in the body; therefore, stopping treatment will not immediately reverse the biological effect of the drug [44]. Due to this pharmacological property, steroid treatment often has to be tapered over several weeks to ensure that the patient's condition does not worsen after halting treatment.
To prevent severe cardiotoxicity in the future, several studies recommend routine cardiac surveillance before starting ICI treatment and within the first 1-4 cycles or up to 12 weeks into treatment [39,44,70]. Lyon et al. recommends testing NT-proBNP, cardiac troponin, and an ECG for this purpose [44]. This surveillance is particularly important in patients with pre-existing cardiac problems [71,72]. In order to carry out this surveillance, baseline cardiac function testing needs to be performed, because patients with preexisting cardiac problems may have high troponin levels due to that disease process rather than ICI cardiotoxicity [73]. Sarocchi et al. report that, during a trial of monitoring troponin levels to predict myocarditis, a few patients developed a small elevation of troponin levels without any symptoms related to this increase; because of this, they postulate that many patients may have subclinical myocarditis [73].

Discussion
Cardiotoxicity, though a rare side effect of immune checkpoint inhibitors, is a concerning one due to its high mortality rate and presentation soon after treatment initiation. The most common cardiotoxicity, myocarditis, has by far the highest mortality rate of all cardiotoxicities. However, if they do not progress to become fatal, these cardiotoxicities often resolve quickly with steroid treatment.
There is much variability in the weeks until cardiotoxicity presentation between the type of cardiotoxicity, the specific antibody, and the type of cancer being treated. As shown by the averages and medians in Tables 2-4, the bell curve of weeks until presentation of cardiotoxicity is positively skewed. This indicates that though the majority of cases present soon after initiation of ICI treatment, there are several cases that have presented as far as 2 years after initiation of treatment. Based on this information, clinicians must be fully vigilant regarding cardiac toxicity in patients soon after treatment initiation. However, the risk of cardiotoxicity never completely disappears; patients may need to be monitored for suspicious symptoms even years after starting ICI treatment.
Between treatments, ipilimumab appears to be the treatment that presents with cardiotoxicity the latest, and ipilimumab + nivolumab patients present in the shortest time (excluding atezolizumab due to lack of corroborating data). It is unclear why this is the case. However, several studies have stated that the PD-1/PD-L1 pathway specifically is important in preventing cardiac autoimmunity [4,5,46,74], so the CTLA-4 pathway may be less important and thus take longer to cause cardiotoxicity. In addition, a combination of ICIs may cause a faster presentation of immune-related adverse events in general due to more widespread blockage of inhibitory signals.
Within cancer types, there is much variability as well, but there does not appear to be a clear pattern in terms of which cancer presents with cardiotoxicity in a shorter or longer timeframe. Within types of cardiotoxicity, however, clearer trends are seen. Patients who present with a combination of cardiotoxicities frequently present very early into treatment as compared to single cardiotoxicities. In addition, myocarditis tends to present in a shorter time frame than many other cardiotoxicity types. It is unclear why this trend appears. Additional research needs to be done to confirm these trends and investigate why this occurs.
Further research also needs to be done on myocardial infarctions and Takotsubo cardiomyopathy in patients taking immune checkpoint inhibitors. These presentations are uncommon but can be fatal, and the timing, histopathological findings, and symptoms of patients with these conditions due to ICI treatment is poorly understood. In addition, very few case reports were found for patients with cardiotoxicity taking durvalumab or atezolizumab; as these drugs become more widely used, investigations into the likelihood of cardiotoxicity with these antibodies need to be carried out.

Conclusions
Immune checkpoint inhibitors may cause several immune-related side effects; one rare side effect is cardiac toxicity, including myocarditis, pericarditis, Takotsubo cardiomyopathy, arrhythmias, and/or myocardial infarction. Though these side effects are rare, they have a high mortality rate; it is important to be aware of the common symptoms and lab results associated with them while treating patients. The best way to treat any cardiac toxicity is usually high doses of steroids; other symptomatic treatments may also be warranted.

Conflicts of Interest:
The authors declare no conflict of interest.

ICI
Immune checkpoint inhibitor IRAE Immune-related adverse event MACE Major adverse cardiac event CMR Cardiovascular magnetic resonance imaging NSCLC Non-small-cell lung cancer Appendix A Table A1. Patients with a wide range of signs and symptoms, from asymptomatic to severe chest pain, dyspnea, multiorgan failure, and sudden death.